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Glucose-6-phosphate dehydrogenase deficiency in the newborn: its prevalence and relation to neonatal jaundice. <i>Southeast Asian J Trop Med Public Health.<\/i> 1995;26(suppl 1):137-141."},{"key":"E00009","doi-asserted-by":"crossref","unstructured":"Panich V. Glucose-6-phosphate dehydrogenase deficiency, 2: tropical Asia. <i>Clin Haematol.<\/i> 1981;10:800-814.","DOI":"10.1016\/S0308-2261(21)00300-3"},{"key":"E00010","unstructured":"Kitayaporn D, Charoenlarp P, Pattaraarechachai J, Pholpoti T. G6PD deficiency and fava bean consumption do not produce hemolysis in Thailand. <i>Southeast Asian J Trop Med Public Health.<\/i> 1991;22:176-182."},{"key":"E00011","unstructured":"Beutler E, Vulliamy TJ. Hematologically important mutations: glucose-6-phosphate dehydrogenase. <i>Blood Cells Mol Dis.<\/i> 2002;28:93-103."},{"key":"E00012","unstructured":"Nuchprayoon I, Sanpavat S, Nuchprayoon S. Glucose-6-phosphate dehydrogenase (G6PD) mutations in Thailand: G6PD Viangchan (871G>A) is the most common deficiency variant in the Thai population. <i>Hum Mutat.<\/i> 2002;19:185-190."},{"key":"E00013","unstructured":"Yang Z, Chu J, Ban G, Huang X, Xu S, Li M. The genotype analysis of glucose-6-phosphate dehydrogenase deficiency in Yunnan province [in Chinese]. <i>Zhonghua Yi Xue Yi Chuan Xue Za Zhi.<\/i> 2001;18:259-263."},{"key":"E00014","unstructured":"Laosombat V, Sattayasevana B, Janejindamai W, et al. Molecular heterogeneity of glucose-6-phosphate dehydrogenase (G6PD) variants in the south of Thailand and identification of a novel variant (G6PD Songklanagarind). <i>Blood Cells Mol Dis.<\/i> 2005;34:191-196."},{"key":"E00015","unstructured":"Standardization of procedures for the study of glucose-6-phosphate dehydrogenase: report of a WHO Scientific Group. <i>World Health Organ Tech Rep Ser.<\/i> 1967;366:1-53."},{"key":"E00016","unstructured":"Huang CS, Hung KL, Huang MJ, Li YC, Liu TH, Tang TK. Neonatal jaundice and molecular mutations in glucose-6-phosphate dehydrogenase deficient newborn infants. <i>Am J Hematol.<\/i> 1996;51:19-25."},{"key":"E00017","unstructured":"Maffi D, Pasquino MT, Caprari P, et al. Identification of G6PD Mediterranean mutation by amplification refractory mutation system. <i>Clin Chim Acta.<\/i> 2002;321:43-47."},{"key":"E00018","unstructured":"Ren X, Du C, Lin Q. 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Haptoglobin therapy for acute favism: a Japanese boy with glucose-6-phosphate dehydrogenase Guadalajara. <i>Br J Haematol.<\/i> 1995;89:421-423."},{"key":"E00028","unstructured":"Panich V, Sungnate T. Characterization of glucose-6-phosphate dehydrogenase in Thailand: the occurrence of 6 variants among 50 G-6-PD deficient Thai. <i>Humangenetik.<\/i> 1973;18:39-46."},{"key":"E00029","unstructured":"Panich V, Na-Nakorn S. G-6-PD variants in Thailand. <i>J Med Assoc Thai.<\/i> 1980;63:537-543."},{"key":"E00030","unstructured":"Chiu DT, Zuo L, Chen E, et al. Two commonly occurring nucleotide base substitutions in Chinese G6PD variants. <i>Biochem Biophys Res Commun.<\/i> 1991;180:988-993."},{"key":"E00031","unstructured":"Chen BH, Lin SR, Chiang CH, Chao MC. Molecular characterization of Chinese G6PD deficiency by using polymerase chain reaction\/single strand conformation polymorphism. <i>Kaohsiung J Med Sci.<\/i> 1998;14:197-202."},{"key":"E00032","unstructured":"Yang Z, Chu J, Xu S, Lin K, Tao Y, Shi L. The preliminary study on the gene mutations of sixty patients with G6PD deficiency in Yunnan province [in Chinese]. <i>Zhonghua Xue Ye Xue Za Zhi.<\/i> 2000;21:509-511."},{"key":"E00033","unstructured":"Liu J, Ren X, Chen Q, et al. Comparative study of three common G6PD gene mutations in Yao and Han People in Guangxi [in Chinese]. <i>Zhonghua Xue Ye Xue Za Zhi.<\/i> 2000;21:190-191."},{"key":"E00034","unstructured":"Du CS, Ren X, Chen L, Jiang W, He Y, Yang M. Detection of the most common G6PD gene mutations in Chinese using amplification refractory mutation system. <i>Hum Hered.<\/i> 1999;49:133-138."},{"key":"E00035","unstructured":"Chang JG, Chiou SS, Perng LI, et al. Molecular characterization of glucose-6-phosphate dehydrogenase (G6PD) deficiency by natural and amplification created restriction sites: five mutations account for most G6PD deficiency cases in Taiwan. <i>Blood.<\/i> 1992;80:1079-1082."},{"key":"E00036","unstructured":"Ainoon O, Joyce J, Boo NY, Cheong SK, Zainal ZA, Hamidah NH. Glucose-6-phosphate dehydrogenase (G6PD) variants in Malaysian Chinese. <i>Hum Mutat.<\/i> 1999;14:352-359."},{"key":"E00037","unstructured":"Saha S, Saha N, Tay JS, Jeyaseelan K, Basair JB, Chew SE. Molecular characterisation of red cell glucose-6-phosphate dehydrogenase deficiency in Singapore Chinese. <i>Am J Hematol.<\/i> 1994;47:273-277."},{"key":"E00038","unstructured":"Panich V, Sungnate T, Wasi P, Na-Nakorn S. G-6-PD Mahidol: the most common glucose-6-phosphate dehydrogenase variant in Thailand. <i>J Med Assoc Thai.<\/i> 1972;55:576-585."},{"key":"E00039","unstructured":"Beutler E, Westwood B, Kuhl W, Hsia YE. Glucose-6-phosphate dehydrogenase variants in Hawaii. <i>Hum Hered.<\/i> 1992;42:327-329."},{"key":"E00040","unstructured":"Iwai K, Hirono A, Matsuoka H, et al. Distribution of glucose-6-phosphate dehydrogenase mutations in Southeast Asia. <i>Hum Genet.<\/i> 2001;108:445-449."},{"key":"E00041","unstructured":"Ainoon O, Yu YH, Amir Muhriz AL, Boo NY, Cheong SK, Hamidah NH. Glucose-6-phosphate dehydrogenase (G6PD) variants in Malaysian Malays. <i>Hum Mutat.<\/i> 2003;21:101-109."},{"key":"E00042","unstructured":"Yusoff NM, Shirakawa T, Nishiyama K, et al. Molecular heterogeneity of glucose-6-phosphate dehydrogenase deficiency in Malays in Malaysia. <i>Int J Hematol.<\/i> 2002;76:149-152."},{"key":"E00043","unstructured":"Beutler E, Westwood B, Kuhl W. Definition of the mutations of G6PD Wayne, G6PD Viangchan, G6PD Jammu, and G6PD \"LeJeune.\" <i>Acta Haematol.<\/i> 1991;86:179-182."},{"key":"E00044","unstructured":"Beutler E, Kuhl W. 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